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FDA 510(k)

CHLAMYDIA TRANSETTEE 1 & 3

K-Number: K823179 · 1982-11-16

ApplicantSpectrum Co.
Decision Date1982-11-16
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CHLAMYDIA TRANSETTEE 1 & 3 is the device name listed in this FDA 510(k) record. The listed applicant is Spectrum Co.. It received FDA 510(k) clearance on 1982-11-16 under 510(k) number K823179. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHLAMYDIA TRANSETTEE 1 & 3?

CHLAMYDIA TRANSETTEE 1 & 3 is a medical device that received FDA 510(k) clearance on 1982-11-16. The listed applicant is Spectrum Co.. The 510(k) number is K823179.

When did CHLAMYDIA TRANSETTEE 1 & 3 receive FDA 510(k) clearance?

CHLAMYDIA TRANSETTEE 1 & 3 received FDA 510(k) clearance on 1982-11-16, under 510(k) number K823179.

Who is the listed applicant for CHLAMYDIA TRANSETTEE 1 & 3?

The FDA 510(k) record lists Spectrum Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHLAMYDIA TRANSETTEE 1 & 3?

The FDA product code for CHLAMYDIA TRANSETTEE 1 & 3 is JSM.

Related Clinical Trials

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Other records listing Spectrum Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K895364LID LOCK874604HISTOBRUSH

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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